N/A
Completed N=107
A Study to Evaluate SimPull for Lateral Patient Transfer
Lateral Patient Transfer
Source: ClinicalTrials.gov NCT05856123 ↗
Enrolled (actual)
107
Serious AEs
0.0%
Results posted
Oct 2025
Primary outcomePrimary: Time to Complete Lateral Transfer — 33.40; 4.094 minutes
Summary
The purpose of this research is to test an investigational device called SimPull to see if it is a more efficient method of transferring a patient from one bed to another compared to that of current methods. The purpose of this research is to gather information on the safety and effectiveness of the SimPull device.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Time to Complete Lateral Transfer |
33.40; 4.094 | — |
| PRIMARY The Number of Staff Involved in a Transfer |
4.98; 4.92 | — |
| PRIMARY Average Weight of Participants |
86.24; 89.47 | — |
| SECONDARY Clinician Satisfaction |
44; 40 | — |
| SECONDARY The Number of Survey Responses From Clinicians Who Indicated They Were Very Likely to Experience Injury During Transfers |
0; 2 | — |
Eligibility Criteria
Inclusion Criteria
- Patients requiring lateral transfer for an invasive cardiac procedure to and from gurney to exam table.
- Patients requiring lateral transfer for an invasive cardiac procedure to and from exam table to gurney.
- Patient does not have compound fractures or cervical fractures present.
- Patient does not have skin damage or open wounds to the dorsal cavity.
- Patient or legally authorized representative (LAR) must be able/present to sign consent.
Exclusion Criteria
- Patients who do not require lateral transfer for an invasive cardiac procedure to and from gurney to exam table.
- Patients who do not require lateral transfer for an invasive cardiac procedure to and from exam table to gurney.
- Patient has compound fractures or cervical fractures present.
- Patient has skin damage or open wounds to the dorsal cavity.
- Patient or legally authorized representative (LAR) are unable/present to sign consent.
Data sourced from ClinicalTrials.gov (NCT05856123). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.